Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 30561–30580 of 49,976 recalls
Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148...
The Issue: Discoloration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLENZIderm M.D. Acne Treatment System Recalled by Valeant Pharmaceuticals...
The Issue: Discoloration.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of...
The Issue: Lack of assurance of sterility: product was found to be empty, under-filled,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinonide Cream UPS Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross contamination with other products: Certain lots of Fluocinonide Cream...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kalbitor (ecallantide) Recalled by Shire Due to Presence of Particulate...
The Issue: Presence of Particulate Matter: Glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation Recalled...
The Issue: Medtronic received reports that the DBS depth stop did not adequately secure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ Administration Set Recalled by Smiths Medical ASD Inc. Due to Smiths...
The Issue: Smiths Medical has become aware that the drawing on the Instructions for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIZA Vertebral Body Replacement Recalled by Eden Spine Europe SA Due to...
The Issue: Complaints that implants have been disassembled by surgeons because of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Estradiol II Recalled by BioMerieux SA Due to Fulvestrant cross reacts...
The Issue: Fulvestrant cross reacts with the VIDAS Estradiol II immunoassay and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrectomy Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ophthalmic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Wischmeier Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dicken Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrectomy Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.